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Nucleosides & Nucleotides|August 26, 1998
Synthesis, antiviral and cytostatic activities of carbocyclic nucleosides incorporating a modified cyclopentane ring. Part 2: Adenosine and uridine analoguesM I Nieto, J M Blanco, O Caamaño, et al.
Cancer Gene Therapy|April 19, 2000
Comparative in vitro and in vivo cytotoxic activity of (E)-5-(2-bromovinyl)-2'-deoxyuridine (BVDU) and its arabinosyl derivative, (E)-5-(2-bromovinyl)-1-beta-D-arabinofuranosyluracil (BVaraU), against tumor cells expressing either the Varicella zoster or the Herpes simplex virus thymidine kinaseC Grignet-Debrus, V Cool, N Baudson, et al.
European Journal of Medicinal Chemistry|August 2, 2011
Acyclic nucleoside thiophosphonates as potent inhibitors of HIV and HBV replicationKarine Barral, Clément Weck, Nadine Payrot, et al.
Bioorganic & Medicinal Chemistry|August 10, 2011
Synthesis and structure-activity relationship of novel diarylpyrimidines with hydromethyl linker (CH(OH)-DAPYs) as HIV-1 NNRTIsShuang-Xi Gu, Qiu-Qin He, Shi-Qiong Yang, et al.
Anticancer Research|June 10, 2019
Long-term Prognostic Impact of Chromosome Abnormalities in Clear Cell Renal Cell CarcinomaCarlotta Palumbo, Maria Furlan, Piera Balzarini, et al.
Journal of Medicinal Chemistry|November 25, 1994
1,2,3-Triazole-[2',5'-bis-O-(tert-butyldimethylsilyl)-beta-D- ribofuranosyl]-3'-spiro-5"-(4"-amino-1",2"-oxathiole 2",2"-dioxide) (TSAO) analogues: synthesis and anti-HIV-1 activityR Alvarez, S Velázquez, A San-Félix, et al.
Nucleosides & Nucleotides|August 5, 1999
Prodrugs of Ara-CMP and Ara-AMP with a S-acyl-2-thioethyl (SATE) biolabile phosphate protecting group: synthesis and biological evaluationR Bazzanini, S Manfredini, E Durini, et al.
Molecular Pharmacology|August 1, 1996
Potent inhibition of human immunodeficiency virus and herpes simplex virus type 1 by 9-(2-phosphonylmethoxyethyl)adenine in primary macrophages is determined by drug metabolism, nucleotide pools, and cytokinesC F Perno, E Balestra, S Aquaro, et al.
Bioorganic & Medicinal Chemistry Letters|August 28, 2003
Improving the selectivity of acyclic nucleoside analogues as inhibitors of human mitochondrial thymidine kinase: replacement of a triphenylmethoxy moiety with substituted amines and carboxamidesAna-Isabel Hernández, Jan Balzarini, Fátima Rodríguez-Barrios, et al.
Chemical Communications (Cambridge, England)|August 18, 2012
New anti-HIV aptamers based on tetra-end-linked DNA G-quadruplexes: effect of the base sequence on anti-HIV activityValentina D'Atri, Giorgia Oliviero, Jussara Amato, et al.
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